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Quatro-M Femoral Stem

FDA UDI

Class II (US FDA UDI)

by Signal Medical Corp.

Identity

Trade Name
Quatro-M Femoral Stem FDA UDI
Generic Name
Press-fit hip femur prosthesis, one-piece FDA UDI
Device Name
Quatro-M Femoral Stem 3L FDA UDI
Model / Reference
3L FDA UDI
Description
Quatro-M Femoral Stem 3L FDA UDI

Identifiers

Catalog Number
WK-1-1015 FDA UDI
Primary DI / UDI-DI
B046WK110150 FDA UDI
510(k) Number
K033313 FDA UDI
FDA Product Code
LWJ FDA UDI
LPH FDA UDI
GMDN Term
Press-fit hip femur prosthesis, one-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3360 FDA UDI
888.3358 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Press-fit hip femur prosthesis, one-piece

Quatro-M Femoral Stem by Signal Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Press-fit hip femur prosthesis, one-piece.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7c9143ea-2223-4275-afe0-4f785e8b83b3 36 fields · synced Jun 1, 2026